A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174146



Internal ID22332670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:78202724..78203750hg38UCSC Ensembl
chrX:77458221..77459247hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg381027
hg191027
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10163n152
Supporting Variantsnssv14455125
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174146
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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